Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism

por Tavasoli, Mahtab, Lahire, Sarah, Sokolenko, Stanislav, Novorolsky, Robyn, Reid, Sarah Anne, Lefsay, Abir, Otley, Meredith O. C., Uaesoontrachoon, Kitipong, Rowsell, Joyce, Srinivassane, Sadish, Praest, Molly, MacKinnon, Alexandra, Mammoliti, Melissa Stella, Maloney, Ashley Alyssa, Moraca, Marina, Pedro Fernandez-Murray, J., McKenna, Meagan, Sinal, Christopher J., Nagaraju, Kanneboyina, Robertson, George S., Hoffman, Eric P., McMaster, Christopher R.
Publicado 2022

A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis

por Ahmed, Mustafa Y, Al-Khayat, Aisha, Al-Murshedi, Fathiya, Al-Futaisi, Amna, Chioza, Barry A, Pedro Fernandez-Murray, J, Self, Jay E, Salter, Claire G, Harlalka, Gaurav V, Rawlins, Lettie E, Al-Zuhaibi, Sana, Al-Azri, Faisal, Al-Rashdi, Fatma, Cazenave-Gassiot, Amaury, Wenk, Markus R, Al-Salmi, Fatema, Patton, Michael A, Silver, David L, Baple, Emma L, McMaster, Christopher R, Crosby, Andrew H
Publicado 2017